Product Recalls in Michigan
Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,722 recalls have been distributed to Michigan in the last 12 months.
Showing 4501–4520 of 53,342 recalls
Recalled Item: SURG STRP 1/4X6 Model/Catalog Number: 801450. The surgical patties and...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURG PAT XRAY 1X1 Model/Catalog Number: 801403. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactaid Lactose Reduced milk 1. 96 oz Lactaid Whole Milk Recalled by HP Hood...
The Issue: Milk may contain undeclared almond from almond milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: Presence of glass particle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...
The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...
The Issue: To better define the drying procedures described in the IFU to improve the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...
The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult Ear Clip SpO2 Sensor Recalled by Nihon Kohden America Inc...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor Recalled by...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed Recalled by Baxter...
The Issue: The beds have a potential for an interface issue with the Rauland Responder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow+ Multi-Test HbA1c System consists of (1) a semi-disposable...
The Issue: The reason for this recall is PTS Diagnostics, Inc. received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atovaquone Oral Suspension Recalled by Bionpharma Inc. Due to Microbial...
The Issue: Microbial Contamination of a Non-sterile Product: The product was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The IMAGEnet 6 Ophthalmic Data System is a software program Recalled by...
The Issue: The overlay of visual field test locations on a probability map, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use...
The Issue: A Gen 5 tail piece was assembled to a Gen 4 Finished Device, resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing...
The Issue: The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P.M. Recalled by AbbVie Inc. Due to Lack of Assurance of Sterility: The...
The Issue: Lack of Assurance of Sterility: The impacted lots may contain a breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACRI-LUBE Recalled by AbbVie Inc. Due to Lack of Assurance of Sterility:...
The Issue: Lack of Assurance of Sterility: The impacted lots may contain a breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.